rs369571363

Variant names:

• chr16-84398538-A-C
• rs369571363
• NM_014861.4:c.139A>C

Your query was ambiguous. Multiple possible variants found:

• chr16-84398538-A-C
• chr16-84398538-A-G
• chr16-84398538-A-T

Variant summary

Our verdict is Uncertain significance. The variant received 0 ACMG points: 2P and 2B. PM2 BP4_Moderate

The NM_014861.4(ATP2C2):​c.139A>C​(p.Lys47Gln) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. 17/22 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Another variant affecting the same amino acid position, but resulting in a different missense (i.e. K47E) has been classified as Uncertain significance.

• Frequency: Genomes: not found (cov: 32)
• Consequence: ATP2C2 NM_014861.4 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 2.61
• Publications: 1 publications found

Genes affected

ATP2C2 (HGNC:29103): (ATPase secretory pathway Ca2+ transporting 2) Enables P-type calcium transporter activity and P-type manganese transporter activity. Predicted to be involved in calcium ion transmembrane transport; cellular calcium ion homeostasis; and manganese ion transport. Predicted to act upstream of or within mammary gland epithelium development; positive regulation of calcium ion import; and protein localization to plasma membrane. Predicted to be located in trans-Golgi network membrane. Predicted to be active in Golgi membrane; endoplasmic reticulum; and plasma membrane. Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Our verdict: Uncertain_significance. The variant received 0 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.078567445).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
ATP2C2	NM_014861.4	c.139A>C	p.Lys47Gln	missense_variant	Exon 2 of 27	ENST00000262429.9	NP_055676.3
ATP2C2	NM_001286527.3	c.139A>C	p.Lys47Gln	missense_variant	Exon 2 of 28		NP_001273456.2
ATP2C2	XM_011523486.3	c.70A>C	p.Lys24Gln	missense_variant	Exon 2 of 28		XP_011521788.1
ATP2C2	XM_047434994.1	c.70A>C	p.Lys24Gln	missense_variant	Exon 2 of 27		XP_047290950.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ATP2C2	ENST00000262429.9	c.139A>C	p.Lys47Gln	missense_variant	Exon 2 of 27	1	NM_014861.4	ENSP00000262429.4
ATP2C2	ENST00000416219.7	c.139A>C	p.Lys47Gln	missense_variant	Exon 2 of 28	1		ENSP00000397925.2

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 30

GnomAD4 genome Cov.: 32

Alfa AF: 0.00 Hom.: 0

Bravo AF: 0.00000378

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.087
BayesDel_addAF	Benign	0.0072	T
BayesDel_noAF	Benign	-0.23
CADD	Benign	19
DANN	Benign	0.86
DEOGEN2	Benign	0.0098	T;.
Eigen	Benign	-0.58
Eigen_PC	Benign	-0.49
FATHMM_MKL	Benign	0.64	D
LIST_S2	Uncertain	0.87	D;D
M_CAP	Benign	0.019	T
MetaRNN	Benign	0.079	T;T
MetaSVM	Uncertain	-0.27	T
MutationAssessor	Benign	0.90	L;L
PhyloP100		2.6
PrimateAI	Benign	0.40	T
PROVEAN	Benign	-0.84	N;N
REVEL	Benign	0.26
Sift	Benign	0.25	T;T
Sift4G	Benign	0.56	T;T
Polyphen		0.29	B;.
Vest4		0.21
MutPred		0.26		Loss of ubiquitination at K47 (P = 0.0141);Loss of ubiquitination at K47 (P = 0.0141);
MVP		0.75
ClinPred		0.56	D
GERP RS		2.8
Varity_R		0.22
gMVP		0.40

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.010		Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs369571363; hg19: chr16-84432144;